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真核生物进化过程中无义介导的mRNA降解复合体成分的保守性

Conservation of Nonsense-Mediated mRNA Decay Complex Components Throughout Eukaryotic Evolution.

作者信息

Causier Barry, Li Zhen, De Smet Riet, Lloyd James P B, Van de Peer Yves, Davies Brendan

机构信息

Centre for Plant Sciences, Faculty of Biological Sciences, University of Leeds, Leeds, LS2 9JT, UK.

Department of Plant Biotechnology and Bioinformatics, Ghent University, Technologiepark 927, B-9052, Gent, Belgium.

出版信息

Sci Rep. 2017 Nov 30;7(1):16692. doi: 10.1038/s41598-017-16942-w.

Abstract

Nonsense-mediated mRNA decay (NMD) is an essential eukaryotic process regulating transcript quality and abundance, and is involved in diverse processes including brain development and plant defenses. Although some of the NMD machinery is conserved between kingdoms, little is known about its evolution. Phosphorylation of the core NMD component UPF1 is critical for NMD and is regulated in mammals by the SURF complex (UPF1, SMG1 kinase, SMG8, SMG9 and eukaryotic release factors). However, since SMG1 is reportedly missing from the genomes of fungi and the plant Arabidopsis thaliana, it remains unclear how UPF1 is activated outside the metazoa. We used comparative genomics to determine the conservation of the NMD pathway across eukaryotic evolution. We show that SURF components are present in all major eukaryotic lineages, including fungi, suggesting that in addition to UPF1 and SMG1, SMG8 and SMG9 also existed in the last eukaryotic common ancestor, 1.8 billion years ago. However, despite the ancient origins of the SURF complex, we also found that SURF factors have been independently lost across the Eukarya, pointing to genetic buffering within the essential NMD pathway. We infer an ancient role for SURF in regulating UPF1, and the intriguing possibility of undiscovered NMD regulatory pathways.

摘要

无义介导的mRNA衰变(NMD)是真核生物中一个重要的过程,可调节转录本的质量和丰度,并参与包括大脑发育和植物防御在内的多种过程。尽管NMD机制的某些部分在不同生物界中是保守的,但人们对其进化了解甚少。核心NMD组分UPF1的磷酸化对NMD至关重要,在哺乳动物中由SURF复合体(UPF1、SMG1激酶、SMG8、SMG9和真核释放因子)调节。然而,据报道真菌和植物拟南芥的基因组中缺少SMG1,因此尚不清楚后生动物之外的UPF1是如何被激活的。我们利用比较基因组学来确定NMD途径在真核生物进化过程中的保守性。我们发现SURF组分存在于所有主要的真核生物谱系中,包括真菌,这表明除了UPF1和SMG1之外,SMG8和SMG9在18亿年前的最后一个真核生物共同祖先中也已存在。然而,尽管SURF复合体起源古老,我们还发现SURF因子在整个真核生物中独立丢失,这表明在关键的NMD途径中存在遗传缓冲。我们推断SURF在调节UPF1方面具有古老的作用,并且存在尚未发现的NMD调节途径这一有趣可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/840f/5709506/18b76d3c3c5b/41598_2017_16942_Fig1_HTML.jpg

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